Reactivation of FMR1 by CRISPR/Cas9-Mediated Deletion of the Expanded CGG-Repeat of the Fragile X Chromosome
Author:
Funder
National Institutes of Health
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
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3. Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locus;RS Alisch;BMC medical genetics,2013
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